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dc.contributor.authorBourret, Emmanuel
dc.contributor.authorStevenson, Steven
dc.contributor.authorCôté, Michel
dc.date.accessioned2024-09-16T11:51:37Z
dc.date.availableNO_RESTRICTIONfr
dc.date.available2024-09-16T11:51:37Z
dc.date.issued2024-07-24
dc.identifier.urihttp://hdl.handle.net/1866/33807
dc.publisherAmerican Chemical Societyfr
dc.subjectCarbonfr
dc.subjectCarbon nanomaterialsfr
dc.subjectMoleculesfr
dc.subjectNanospheresfr
dc.subjectPolarizabilityfr
dc.titleAnisotropic contributions in the chromatographic elution behavior of fullerenes and fullertubesfr
dc.typeArticlefr
dc.contributor.affiliationUniversité de Montréal. Faculté des arts et des sciences. Département de physiquefr
dc.identifier.doi10.1021/acs.jpcc.4c02931
dcterms.abstractThe retention behavior of fullerenes and fullertubes on a PYE column in reversed-phase chromatography was investigated to clarify the influence of their shapes on the separation process. The impact of anisotropy was further elucidated using a pair potential interaction model, together with experimental data and ab initio calculations, to evaluate its contribution to various parameters characterizing the interaction models. The findings indicate that the shape of fullerenes plays a more significant role than anticipated in the retention mechanisms, highlighting the necessity of considering the shape of fullerenes and fullertubes to accurately predict their retention times. Furthermore, a phenomenological pair potential was devised to demonstrate the feasibility of precisely predicting the retention times of fullerenes and fullertubes through first-principles calculations, regardless of their shape. The existence of such a model paves the way for the development of a method to identify isomers of fullerenes from minute amounts of sample.fr
dcterms.isPartOfurn:ISSN:1932-7447fr
dcterms.isPartOfurn:ISSN:1932-7455fr
dcterms.languageengfr
UdeM.ReferenceFournieParDeposanthttps://doi.org/10.1021/acs.jpcc.4c02931fr
UdeM.VersionRioxxVersion acceptée / Accepted Manuscriptfr
oaire.citationTitleJournal of physical chemistry Cfr
oaire.citationVolume128fr
oaire.citationIssue31fr
oaire.citationStartPage13283fr
oaire.citationEndPage13298fr


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